Abstract
Rabbit bone-marrow macrophages and fibroblasts were cultured, independently or together, with pieces of 35S-labelled cartilage or at the surface of dried [14C]collagen gels. Each type of cell, cultivated alone, rapidly degraded the proteoglycan of cartilage, but only the fibroblasts degraded collagen. The co-culture of both types of cell had no consistent effect on the rate of proteoglycan degradation, but it stimulated the rate of collagen degradation. In parallel, the accumulation of collagenase in the culture fluid was enhanced but not that of neutral proteinase. Coinditioned media from macrophage cultures added to cultures of fibroblasts had the same effect as the living macrophages in stimulating the production of collagenase. Their action was itself enhanced when the macrophages had been activated by concanavalin A-stimulated spleen-cell factors. These data suggest that fibroblasts may act as effector cells in producing collagenase and degrading collagen in response to soluble factors released by macrophages under the control of lymphocyte factors.
MeSH Terms
Animals
Bone Marrow/enzymology
Cartilage/metabolism
Cells, Cultured
Collagen/metabolism
Culture Media
Fibroblasts/enzymology
Interleukin-2/pharmacology
Macrophages/drug effects,enzymology
Male
Microbial Collagenase/biosynthesis
Peptide Hydrolases/biosynthesis
Rabbits
Chemicals
Culture Media
Interleukin-2
Collagen
Peptide Hydrolases
Microbial Collagenase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Huybrechts-Godin G
Hauser P
Vaes G
References (18)
18 references, click to expand
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